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. 2011 Aug 17;301(6):C1325–C1343. doi: 10.1152/ajpcell.00054.2011

Fig. 8.

Fig. 8.

Pharmacological profiles of Rb+ influx and lithium uptake into oocytes expressing wild-type RhAG or RhAG F65S. A: effects of inhibitors on 86Rb+ influx into Xenopus oocytes expressing wild-type RhAG. B: effects of inhibitors on 86Rb+ influx into oocytes expressing RhAG F65S. C: effects of inhibitors on Li+ influx into oocytes expressing wild-type RhAG. D: effects of inhibitors on Li+ influx into oocytes expressing RhAG F65S. Values are means ± SE for (n) oocytes. Inhibitor concentrations were DIDS (500 μM), amiloride (1 mM), NH4Cl (5 mM), methylammonium (MA; 5 mM), phloretin (500 μM), and Gd3+ (50 μM). Ouabain (0.5 mM) and bumetanide (5 μM) were present in all experiments. *P < 0.05 (gray bar) compared with absence of inhibitor (Dunnett's t-test). Inhibitor effects on uninjected oocytes are summarized in results.